Related gene-specific medical variations for Gene (Select 83953) - ClinVar - NCBI

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Items: 12

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3278255	NM_001170631.2(FCAMR):c.614A>G (p.Asn205Ser)	FCAMR, LOC126805992 (N205S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093909	NM_001170631.2(FCAMR):c.561A>C (p.Gln187His)	FCAMR, LOC126805992 (Q142H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093907	NM_001170631.2(FCAMR):c.497A>G (p.Tyr166Cys)	FCAMR, LOC126805992 (Y166C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093906	NM_001170631.2(FCAMR):c.445A>G (p.Arg149Gly)	FCAMR, LOC126805992 (R149G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093905	NM_001170631.2(FCAMR):c.431G>A (p.Arg144His)	FCAMR, LOC126805992 (R144H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2616947	NM_001170631.2(FCAMR):c.605G>C (p.Ser202Thr)	FCAMR, LOC126805992 (S202T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2592735	NM_001170631.2(FCAMR):c.364G>A (p.Ala122Thr)	FCAMR, LOC126805992 (A122T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2491748	NM_001170631.2(FCAMR):c.380G>A (p.Cys127Tyr)	FCAMR, LOC126805992 (C127Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2381768	NM_001170631.2(FCAMR):c.505C>T (p.Arg169Cys)	FCAMR, LOC126805992 (R169C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2306963	NM_001170631.2(FCAMR):c.629G>A (p.Ser210Asn)	FCAMR, LOC126805992 (S210N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2301495	NM_001170631.2(FCAMR):c.494G>A (p.Arg165His)	FCAMR, LOC126805992 (R165H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2277853	NM_001170631.2(FCAMR):c.437G>A (p.Gly146Glu)	FCAMR, LOC126805992 (G146E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance